- Fabry Disease: Nine New Mutations in alpha-Galactosidase A Gene and Molecular Carrier Detection2001 | First Faculty of Medicine
- Fabry Disease: Ten New Mutations in alpha-Galactosidase A Gene and Molecular Carrier DetectionPublication without faculty affiliation
- Recurrence of Fabry disease as a result of paternal germline mosaicism for alpha-galactosidase A gene mutation2005 | First Faculty of Medicine
- Relationship between X-inactivation and clinical involvement in Fabry heterozygotes. Eleven novel mutations in the alpha-galactosidase A gene in the Czech and Slovak population2005 | First Faculty of Medicine
- Time to treatment benefit for adult patients with Fabry disease receiving agalsidase beta: Data from the Fabry Registry2016 | First Faculty of Medicine
- Characterization of Early Disease Status in Treatment-Naive Male Paediatric Patients with Fabry Disease Enrolled in a Randomized Clinical Trial2015 | First Faculty of Medicine
- The influence of environmental stresses on mutability of Bacillus subtilis - Role of mismatch-repair2009 | Faculty of Science
- Three-dimensional echocardiographic left ventricular strain analysis in Fabry disease: correlation with heart failure severity, myocardial scar, and impact on long-term prognosis2023 | First Faculty of Medicine
- Nationwide screening for Fabry disease in unselected stroke patients2021 | First Faculty of Medicine, Second Faculty of Medicine, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové